Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0233763
Disease: Hallucinations, Visual
Hallucinations, Visual 		39 5 11 7.3E-02 2 2.4E-02
CUI: C0037763
Disease: Spasm
Spasm 		172 0 20 7.3E-02 0 0
CUI: C0005747
Disease: Blepharospasm
Blepharospasm 		44 0 11 7.1E-02 0 0
CUI: C0012569
Disease: Diplopia
Diplopia 		75 0 13 7.1E-02 0 0
CUI: C1843921
Disease: Postural instability
Postural instability 		60 0 12 7.1E-02 0 0
CUI: C0011253
Disease: Delusions
Delusions 		62 0 12 7.0E-02 0 0
CUI: C1839780
Disease: FRAGILE X TREMOR/ATAXIA SYNDROME
FRAGILE X TREMOR/ATAXIA SYNDROME 		62 0 12 7.0E-02 0 0
CUI: C0087012
Disease: Ataxia, Spinocerebellar
Ataxia, Spinocerebellar 		156 0 18 6.9E-02 0 0
CUI: C0752124
Disease: Spinocerebellar Ataxia Type 6 (disorder)
Spinocerebellar Ataxia Type 6 (disorder) 		64 0 12 6.9E-02 0 0
CUI: C0029227
Disease: Delirium, Dementia, Amnestic, Cognitive Disorders
Delirium, Dementia, Amnestic, Cognitive Disorders 		83 0 13 6.8E-02 0 0
CUI: C0543859
Disease: Amyotrophic Lateral Sclerosis, Guam Form
Amyotrophic Lateral Sclerosis, Guam Form 		36 0 10 6.8E-02 0 0
CUI: C0021125
Disease: Impulsive Behavior
Impulsive Behavior 		276 0 25 6.7E-02 0 0
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		362 247 30 6.6E-02 4 1.2E-02
CUI: C0085623
Disease: Akinesia
Akinesia 		43 3 10 6.5E-02 1 1.2E-02
CUI: C0349204
Disease: Nonorganic psychosis
Nonorganic psychosis 		376 98 30 6.4E-02 2 1.1E-02
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
Frontotemporal Lobar Degeneration 		195 54 19 6.4E-02 2 1.5E-02
CUI: C0027746
Disease: Nerve Degeneration
Nerve Degeneration 		165 0 17 6.3E-02 0 0
CUI: C0001956
Disease: Alcohol Use Disorder
Alcohol Use Disorder 		218 0 20 6.2E-02 0 0
CUI: C0393593
Disease: Dystonia Disorders
Dystonia Disorders 		167 0 17 6.2E-02 0 0
CUI: C1846865
Disease: Substantia nigra gliosis
Substantia nigra gliosis 		14 0 8 6.2E-02 0 0
CUI: C1961835
Disease: Gaucher Disease, Type 1
Gaucher Disease, Type 1 		48 124 10 6.2E-02 1 5.0E-03
CUI: C4087347
Disease: Autosomal dominant cerebellar ataxia
Autosomal dominant cerebellar ataxia 		31 0 9 6.2E-02 0 0
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders 		389 0 30 6.2E-02 0 0
CUI: C4275179
Disease: Young onset Parkinson disease
Young onset Parkinson disease 		51 32 10 6.1E-02 5 4.7E-02
CUI: C0751265
Disease: Learning Disabilities
Learning Disabilities 		103 0 13 6.1E-02 0 0